Kumar Yekula Kiran, Rajan Yadavalli R D
Department of General Surgery, Siddhartha Medical College, Vijayawada, Andhra Pradesh, India.
Ann Maxillofac Surg. 2024 Jul-Dec;14(2):252-254. doi: 10.4103/ams.ams_53_23. Epub 2024 Oct 23.
Intraparotid facial nerve schwannoma (IPFNS) is a rare entity. Diagnosing these tumours is challenging as multiple differential diagnoses exist for swellings in the infraauricular region. Delay in diagnosis can lead to adverse outcomes.
A 27-year-old female presented with swelling over the left infraauricular region, which concerned her cosmetic appearance.
It was initially misdiagnosed with imaging techniques computerised tomography (CT scan) and fine-needle aspiration cytology, leading to a diagnostic dilemma.
Superficial parotidectomy was planned and intraoperatively, a cystic lesion was seen adherent to the temporal branch of the facial nerve, which was resected along with the nerve branch. Histopathology confirmed the diagnosis as facial nerve schwannoma.
The patient's cosmetic concern was resolved but there was loss of wrinkles over the ipsilateral forehead region. No recurrence was seen.
TAKE-AWAY LESSONS: IPFNS often causes a diagnostic dilemma and an appropriate and timely diagnosis is required to decrease the morbidity and undertreatment.
腮腺内面神经鞘瘤(IPFNS)是一种罕见的疾病。由于耳下区域肿胀存在多种鉴别诊断,诊断这些肿瘤具有挑战性。诊断延迟可能导致不良后果。
一名27岁女性因左耳下区域肿胀就诊,这影响了她的外貌。
最初通过计算机断层扫描(CT扫描)和细针穿刺细胞学检查进行了误诊,导致诊断陷入困境。
计划进行腮腺浅叶切除术,术中发现一个囊性病变附着于面神经颞支,将其与神经分支一并切除。组织病理学确诊为面神经鞘瘤。
患者对外貌的担忧得到解决,但同侧前额区域出现皱纹消失。未见复发。
IPFNS常导致诊断困境,需要进行恰当及时的诊断以降低发病率和治疗不足的情况。